Package 71872-7296-1

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7296-1
Digits Only 7187272961
Product NDC 71872-7296
Description

1 VIAL, MULTI-DOSE in 1 BAG (71872-7296-1) / 5 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2022-08-10
Brand ketamine hydrochloride
Generic ketamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "fa1d55d6-9b8f-40b4-e053-6294a90ac40e", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238083"], "spl_set_id": ["ea600f8a-857f-4e0e-e053-2995a90a017d"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7296-1)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7296-1", "marketing_start_date": "20220810"}], "brand_name": "Ketamine Hydrochloride", "product_id": "71872-7296_fa1d55d6-9b8f-40b4-e053-6294a90ac40e", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "71872-7296", "dea_schedule": "CIII", "generic_name": "Ketamine Hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketamine Hydrochloride", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA074549", "marketing_category": "ANDA", "marketing_start_date": "20041130", "listing_expiration_date": "20261231"}